Film Breakdown and Nano-Porous Mg(OH)2 Formation from Corrosion of Magnesium Alloys in Salt Solutions

被引:137
作者
Brady, M. P. [1 ]
Rother, G. [1 ]
Anovitz, L. M. [1 ]
Littrell, K. C. [1 ]
Unocic, K. A. [1 ]
Elsentriecy, H. H. [1 ,2 ]
Song, G. -L. [1 ]
Thomson, J. K. [1 ]
Gallego, N. C. [1 ]
Davis, B. [3 ]
机构
[1] Oak Ridge Natl Lab, Oak Ridge, TN 37831 USA
[2] Cent Met Res & Dev Inst, Cairo 11421, Egypt
[3] Magnesium Elektron North Amer, Madison, IL 62060 USA
关键词
SMALL-ANGLE SCATTERING; VIBRATING ELECTRODE TECHNIQUE; ENHANCED CATALYTIC-ACTIVITY; PURE MAGNESIUM; MG ALLOY; LOCALIZED CORROSION; AUTOMOTIVE APPLICATIONS; ANODIC-DISSOLUTION; SULFATE-SOLUTIONS; HYDROGEN STORAGE;
D O I
10.1149/2.0171504jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Small angle neutron scattering (SANS) and scanning transmission electron microscopy (STEM) were used to study film formation by magnesium alloys AZ31B (Mg-3Al-1Zn base) and ZE10A (Elektron 717, E717: Mg-1Zn + Nd, Zr) in H2O and D2O with and without 1 or 5 wt% NaCl. No SANS scattering changes were observed after 24 h D2O or H2O exposures compared with as-received (unreacted) alloy, consistent with relatively dense MgO-base film formation. However, exposure to 5 wt% NaCl resulted in accelerated corrosion, with resultant SANS scattering changes detected. The SANS data indicated both particle and rough surface (internal and external) scattering, but with no preferential size features. The films formed in 5 wt% NaCl consisted of a thin, inner MgO-base layer, and a nano-porous and filamentous Mg(OH)(2) outer region tens of microns thick. Chlorine was detected extending to the inner MgO-base film region, with segregation of select alloying elements also observed in the inner MgO, but not the outer Mg(OH)(2). Modeling of the SANS data suggested that the outer Mg(OH)(2) films had very high surface areas, consistent with loss of film protectiveness. Implications for the NaCl corrosion mechanism, and the potential utility of SANS for Mg corrosion, are discussed. (C) The Author(s) 2015. Published by ECS. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 License (CC BY, http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse of the work in any medium, provided the original work is properly cited. All rights reserved.
引用
收藏
页码:C140 / C149
页数:10
相关论文
共 74 条
[1]   Characterization of ceramics by X-ray and neutron small-angle scattering [J].
Allen, AJ .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 2005, 88 (06) :1367-1381
[2]   Solid-liquid equilibria of Mg(OH)2(cr) and Mg2(OH)3Cl•4H2O(cr) in the system Mg-Na-H-OH-O-Cl-H2O at 25°C [J].
Altmaier, M ;
Metz, V ;
Neck, V ;
Müller, R ;
Fanghänel, T .
GEOCHIMICA ET COSMOCHIMICA ACTA, 2003, 67 (19) :3595-3601
[3]  
[Anonymous], 2013, P 38 WORKSH GEOTH RE
[4]  
Anovitz L. M., 2011, P 36 WORKSH GEOTH RE
[5]   The corrosion of pure magnesium in aerated and deaerated sodium sulphate solutions [J].
Baril, G ;
Pébère, N .
CORROSION SCIENCE, 2001, 43 (03) :471-484
[6]   Evidence for enhanced catalytic activity of magnesium arising from anodic dissolution [J].
Birbilis, N. ;
King, A. D. ;
Thomas, S. ;
Frankel, G. S. ;
Scully, J. R. .
ELECTROCHIMICA ACTA, 2014, 132 :277-283
[7]  
Blawert C, 2004, T INDIAN I METALS, V57, P397
[8]   Tracer Film Growth Study of Hydrogen and Oxygen from the Corrosion of Magnesium in Water [J].
Brady, M. P. ;
Fayek, M. ;
Elsentriecy, H. H. ;
Unocic, K. A. ;
Anovitz, L. M. ;
Keiser, J. R. ;
Song, G. L. ;
Davis, B. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2014, 161 (09) :C395-C404
[9]  
Brunauer S., 1938, Journal of American Chemical Society
[10]  
Cano Z. P., 2014, CORROSION IN PRESS